Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal eye physiology (HP:0012373)

Parent Node:
Abnormal eyelid physiology (HP:0031879)

..Starting node
..Eyelid laxity (HP:0031880)

Term ID:

31880

Name:

Eyelid laxity

Synonym:

Lid laxity

Definition:

Abnormally lax eyelid associated with tissue relaxation; it can be demonstrated by the eyelid distraction test and/or the eyelid snap test.

Comments:

Reference:

HP:0031880

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal eyelid movement (HP:0031785)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031880	HP:0031880	Eyelid laxity	0	CL E G H
HP:0031880	HP:0032029	Floppy eyelid	1	CL E G H
HP:0031880	HP:0032035	Lower eyelid laxity	1	CL E G H
HP:0031880	HP:0032034	Upper eyelid laxity	1	CL E G H
HP:0031880	HP:0032033	Vertical eyelid laxity	1	CL E G H
HP:0031880	HP:0032032	Horizontal eyelid laxity	1	CL E G H
HP:0031880	HP:0032031	Medial canthal tendon laxity	1	CL E G H
HP:0031880	HP:0032030	Lateral canthal tendon laxity	1	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.